Additive and method for removal of impurities formed due to sulfur compounds in crude oils containing calcium naphthenate

ABSTRACT

An additive capable of avoiding formation of impurities and capable of removing or dissolving impurities formed and accumulated at the interphase of organic and aqueous layers on reaction between calcium naphthenate and sulfur compound including H 2 S in presence of water in mixture of crude oils containing calcium naphthenate and sulfur compound or H 2 S, wherein the additive is glyoxylic acid is provided. A method for avoiding formation of impurities and for removing or dissolving impurities formed and accumulated at the interphase of organic and aqueous layers on reaction between calcium naphthenate and sulfur compound including H 2 S in presence of water in mixture of crude oils containing calcium naphthenate and sulfur compound including H 2 S, comprising treating mixture of crude oils containing calcium naphthenate and sulfur compound or H 2 S with glyoxylic acid is also provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a filing under 35 U.S.C. 371 of InternationalApplication No. PCT/IN2010/000858 filed Dec. 28, 2010, entitled“Additive And Method For Removal Of Impurities Formed Due To SulfurCompounds In Crude Oils Containing Calcium Naphthenate,” which claimspriority to Indian Patent Application No. 3050/MUM/2009 filed on Dec.31, 2009, which applications are incorporated by reference herein intheir entirety.

FIELD OF THE INVENTION

The present invention relates to an additive and method for removal ofimpurities formed due to reaction between sulfur compounds, such ashydrogen sulfide [H₂S] and calcium naphthenate in a mixture of crudeoils containing calcium naphthenate and sulfur compounds.

Particularly, the present invention relates to an additive and methodfor removal of impurities formed due to reaction between sulfurcompounds, such as hydrogen sulfide [H₂S] and calcium naphthenate inpresence of water in a mixture of crude oils containing calciumnaphthenate and sulfur compounds.

BACKGROUND OF THE INVENTION

The DOBA is a high acid crude oil originating from the Chad region ofWest Africa. The DOBA is known to contain calcium naphthenate and theamount of calcium naphthenate varies over a range from about 150 toabout 700 ppm. In a typically supplied DOBA crude oil, the amount ofcalcium naphthenate may vary from about 250-about 300 ppm.

The DOBA is a heavy high acid crude oil with Total Acid Number [TAN]ranging upwards of 4.0 mg KOH/gm of sample and the American PetroleumInstitute (API) gravity is about 19. However, the sulfur content in DOBAis very low to nil.

The DOBA is typically a crude oil with a lot of residue in it and forproper blending, typically internationally, refiners blend it with verylight crude oil or condensates to increase the API of the resulted blendto more than 30. Such blending with light crude oil or condensates helpsto create sufficient light ends to help achieve product yields for thecrude distillation unit. The most of light crude oil or condensates thusselected generally have very little to nil sulfur contents or existentand potential H₂S, which means the overall sulfur content still remainsvery low. Further, the H₂S being oil soluble is not present inrelatively higher quantities in these types of blends.

The inventor has observed when DOBA or its above described blendscontaining calcium naphthenate, but having sulfur contents or H₂S beingless than 0.2% is treated with additives as known in the art, forexample with glycolic acid [US patent publication No. 2009/0152164 andU.S. Pat. No. 7,497,943—(US'943)], the presence of low amounts of sulfurin DOBA crude oil or its blends does not produce impurity, and hence,does not hamper removal of metals including calcium from such DOBA crudeoil or its blends.

However, if the refiner processes the DOBA or its blends having APIvarying between about 24 to about 29 and a crude oil having sulfur orH₂S contents in higher amounts as compared to above situation, thepresence of higher amounts of sulfur or H₂S contents in presence ofwater will have first chance to react with calcium naphthenate and as aresult several reactions occur, which have been found to produceinsoluble and soluble impurities, wherein the insoluble impurities getaccumulated in the form of a black layer at the interphase of organicand aqueous layers during isolation of metals including calcium from theDOBA or its blends. The formation of impurities due to reactions betweencalcium naphthenate and sulfur compounds or H₂S in presence of water andtheir accumulation at the interphase of organic and aqueous layers hasbeen found not only to hamper processing of crude oils, but also theremoval of metals including calcium.

The inventor of present invention has observed that if solution ofcalcium naphthenate in an organic solvent, for example toluene havingconcentration of Ca of about 2247 ppm is treated with equal weight ofwater by heating to about 130 degree C., that is, in absence of sulfurcompound or H₂S in a Parr autoclave under autogenous pressure, andseparated into organic and aqueous layers in a separating funnel, noblack layer is formed at the interphase which indicates that calciumnaphthenate does not hydrolyze in absence of sulfur compound or H₂S,which also indicates that no impurities are formed which could haveaccumulated at the interphase. When organic layer, as separated, wasdried by evaporating toluene, its acid value was found to be very low ofabout 48.36 (mg KOH per gm) which also indicates that calciumnaphthenate did not hydrolyze meaning thereby the calcium is not removedfrom the oil. When IR of dried organic material was taken, as shown inaccompanying FIG. 1, presence of peaks at about 1555.3 cm⁻¹ and at about1678.7 cm⁻¹ also indicates that calcium naphthenate did not hydrolyze inabsence of sulfur or H₂S meaning thereby the calcium is not removed fromthe oil. In the description herein, this experiment may be referred asexperiment 1.

When solution of calcium naphthenate in toluene having concentration ofCa of about 2247 ppm and saturated with H₂S [or sulfur compound] bypurging H₂S in a manner to have concentration of H₂S in the vapour phaseof about 13 vol % was treated with equal weight of water by heating toabout 130 degree C., that is, in presence of sulfur compound or H₂S, inParr autoclave under autogenous pressure, calcium naphthenate was foundto react with H₂S [or sulfur compound] in presence of water and onseparation of organic and aqueous layers after cooling to roomtemperature in a separating funnel, a black layer was formed at theinterphase which indicated that calcium naphthenate gets hydrolyzed inpresence of H₂S [or sulfur compound] and water, and impurities formedthereby get accumulated at the interphase. When organic layer, asseparated, was dried by evaporating toluene, its acid value was found tobe high of about 156.26 (mg KOH per gm) which also indicated thatcalcium naphthenate got hydrolyzed meaning thereby calcium is removedfrom the calcium naphthenate in oil or hydrocarbon. When IR of driedorganic material was taken, as shown in accompanying FIG. 2, presence ofweak peak at 1535.7 cm⁻¹ and no peak at 1680.7 cm⁻¹, but strong peak at1696.2 cm⁻¹ in the IR spectrum also indicated that calcium naphthenateis hydrolyzed in presence of H₂S [or sulfur compound] and water meaningthereby calcium is removed from the calcium naphthenate in oil orhydrocarbon. In the description herein, this experiment may be referredas experiment 2.

When experiment 2 was repeated in a manner to have concentration of H₂Sin the vapour phase of about 5 vol % to see if the lower concentrationof H₂S also results in formation of impurities and their accumulation atthe interphase, it was found that even at lower concentration of 5 vol %of H₂S impurities are formed and get accumulated at the interphase evenfor the period up to 60 min. In the description herein, this experimentmay be referred as experiment 2A. The calcium concentration in theorganic layer, as measured by Inductive coupled plasma (ICP) and acidvalue (AV) of the compound obtained after drying the organic layer areprovided against time in the Table-I, which indicate that only up to39.9% of Ca is removed without any additive:

TABLE I Sr. Acid Value % Efficiency Ca Conc. % Efficiency No. Time(MgKOH/gm) (by AV) (ppm) (by Ca) 1  5 min 60.05 26.1 1617 28 2 15 min66.97 29.6 1545 31.2 3 30 min 77.62 33.7 1465 34.8 4 60 min 88.33 38.41350 39.9

Accordingly, the industry processing DOBA or its blend containingcalcium naphthenate and a crude oil containing sulfur compounds or H₂Sfaces problems of formation of impurities upon reaction of calciumnaphthenate and sulfur compounds or H₂S in presence of water for examplewhen such crude oils are processed through desalter and such impuritiescontinue to get accumulated in the system which not only hampersprocessing of crude oils, but also adversely effect removal of metalsincluding calcium.

Problem to be Solved by the Invention

Therefore, problem to be solved is to provide an additive and method forremoval of impurities formed due to reaction between sulfur compounds,such as hydrogen sulfide [H₂S] and calcium naphthenate in presence ofwater in a mixture of crude oils containing calcium naphthenate andsulfur compounds, such as hydrogen sulfide [H₂S].

With above aim, the inventor has tried to solve above industrial problemwith additives known in the prior art, and found that when solution ofcalcium naphthenate in toluene and purged with H₂S as prepared inexperiment 2 was treated in same manner as in experiment 2, but withequal weight of water containing prior art additive—citric acid (C3alpha-hydroxy-tricarboxylic acid), impurities were still formed and gotaccumulated as black layer at the interphase indicating that calciumnaphthenate does hydrolyze in presence of H₂S [or sulfur compound] andwater, but citric acid additive was ineffective in avoiding formation ofimpurities, and thereby, in accumulation of black layer at theinterphase. The acid value of about 229.36 (mg KOH per gm) of separatedand dried organic layer, and no peak at 1538 cm⁻¹ and at 1680.7 cm⁻¹,but strong peak at 1698.7 cm⁻¹ in its IR spectra, as shown inaccompanying FIG. 3, were also indicative of hydrolysis of calciumnaphthenate. In the description herein, this experiment may be referredto as experiment 3.

When experiment 3 was repeated with concentration of H₂S in the vapourphase of about 5 vol % to see if citric acid additive is effective toavoid formation of impurities and their accumulation at the interphase,it was found that even at lower concentration of 5 vol % of H₂S, thecitric acid additive was ineffective in avoiding formation of impuritiesand their accumulation at the interphase even when organic layer hasbeen treated for a period up to 60 min. In the description herein, thisexperiment may be referred as experiment 3A. The calcium concentrationin the organic layer, as measured by ICP and AV of the compound obtainedafter drying the organic layer are provided against time in theTable-II, which indicate that citric acid may be effective in removingthe calcium, but it has not been found to be effective in avoidingformation of impurities and their accumulation at the interphase evenwhen hydrocarbon layer is treated for a period up to 60 min:

TABLE II Sr. Acid Value % Efficiency Ca Conc. % Efficiency No. Time(MgKOH/gm) (by AV) (ppm) (by Ca) 1  5 min 203.14 88.3 42 98.13 2 15 min208.38 90.6 38 98.31 3 30 min 222.43 96.7 36 98.40 4 60 min 221.79 96.430 98.6

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in experiment 2 was treated in same manner as in experiment 2,but with equal weight of water containing prior art additive—maleicanhydride, the impurities were still formed and got accumulated as denseblack layer at the interphase indicating that calcium naphthenate doeshydrolyze in presence of H₂S [or sulfur compound] and water, but maleicanhydride additive was also ineffective in avoiding formation ofimpurities, and thereby, in accumulation of black layer at theinterphase. The acid value of about 216.18 (mg KOH per gm) of separatedand dried organic layer, and no peak at 1538 cm⁻¹ and at 1680.7 cm⁻¹,but strong peak at 1698.9 cm⁻¹ in its IR spectra, as shown inaccompanying FIG. 4, were also indicative of hydrolysis of calciumnaphthenate. In the description herein, this experiment may be referredto as experiment 4.

When experiment 4 was repeated with concentration of H₂S in the vapourphase of about vol % to see if maleic anhydride additive is effective toavoid formation of impurities and their accumulation at the interphase,it was found that even at lower concentration of 5 vol % of H₂S, themaleic anhydride additive was ineffective in avoiding formation ofimpurities and their accumulation at the interphase even when organiclayer has been treated for a period up to 60 min. In the descriptionherein, this experiment may be referred as experiment 4A. The calciumconcentration in the organic layer, as measured by ICP, and AV of thecompound obtained after drying the organic layer are provided againsttime in the Table-III, which indicate that maleic anhydride additive maybe effective in removing the calcium, but it has not been found to beeffective in avoiding formation of impurities and their accumulation atthe interphase even when hydrocarbon layer is treated for a period up to60 min:

TABLE III Sr. Acid Value % Efficiency Ca Conc. % Efficiency No. Time(MgKOH/gm) (by AV) (ppm) (by Ca) 1  5 min 212.25 92.3 77 96.57 2 15 min205.66 89.4 93 95.86 3 30 min 207.34 90.1 77 96.88 4 60 min 214.88 93.4214 90.48

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in experiment 2 was treated in same manner as in experiment 2,but with equal weight of water containing prior art additive—glycolicacid in stoichometric equivalent to calcium concentration, theimpurities were still formed and got accumulated as black layer at theinterphase of organic and aqueous layers indicating that calciumnaphthenate does hydrolyze in presence of H₂S [or sulfur compound] andwater, but glycolic acid additive was also ineffective in avoidingformation of impurities, and thereby, in accumulation of black layer atthe interphase. The acid value of about 214.6 (mg KOH per gm) ofseparated and dried organic layer, and no peak at 1538 cm⁻¹ and at1680.7 cm⁻¹, but strong peak at 1698.8 cm⁻¹ in its IR spectra, as shownin accompanying FIG. 5, were also indicative of hydrolysis of calciumnaphthenate. In the description herein, this experiment may be referredto as experiment 5.

When experiment 5 was repeated with concentration of H₂S in the vapourphase of about 5 vol % to see if glycolic acid additive is effective toavoid formation of impurities and their accumulation at the interphase,it was found that even at lower concentration of 5 vol % of H₂S, theglycolic acid additive was ineffective in avoiding formation ofimpurities and their accumulation at the interphase even when organiclayer has been treated for a period up to 60 min. In the descriptionherein, this experiment may be referred as experiment 5A. The calciumconcentration in the organic layer, as measured by ICP, and AV of thecompound obtained after drying the organic layer are provided againsttime in the Table-IV, which indicate that glycolic acid additive may beeffective in removing the calcium, but it has not been found to beeffective in avoiding formation of impurities and their accumulation atthe interphase even when hydrocarbon layer is treated for a period up to60 min:

TABLE IV Sr. Acid Value % Efficiency Ca Conc. % Efficiency No. Time(MgKOH/gm) (by AV) (ppm) (by Ca) 1  5 min 191.31 83.2 245 89.1 2 15 min193.29 84.0 183 91.9 3 30 min 199.0 86.5 130 94.2 4 60 min 199.5 86.7180 92.0

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in experiment 2 was treated in same manner as in experiment 2with equal weight of water, the impurities were formed and gotaccumulated as dense black layer at the interphase indicating thatcalcium naphthenate does hydrolyze in presence of H₂S [or sulfurcompound] and water. The aqueous layer was carefully drained and priorart additive—glycolic acid in stoichometric equivalent to calcium wasdissolved in this separated aqueous layer, which is then transferredback to the separating funnel containing organic and black layers, andthe contents were vigorously shaken. It was observed that black layerformed did not get disappeared or dissolved, which confirms thatadditive glycolic acid was not effective in dissolving the impuritieswhich had got accumulated as black layer at the interphase. The acidvalue of about 231.53 (mg KOH per gm) of separated and dried organiclayer, and no peak at 1538 cm⁻¹ and at 1680.7 cm⁻¹, but strong peak at1699.0 cm⁻¹ in its IR spectra, as shown in accompanying FIG. 6, werealso indicative of hydrolysis of calcium naphthenate. In the descriptionherein, this experiment may be referred to as experiment 6. It may benoted that this experiment was also performed by direct addition ofaqueous solution of additive glycolic acid after accumulation of blacklayer at the interphase, and found that black layer did not dissolve ordisappear indicating that glycolic acid was not effective in removing ordissolving black layer formed by accumulation of impurities at theinterphase.

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in experiment 2 was treated in same manner as in experiment 2,but with equal weight of water containing additive—DL-malic acid instoichometric equivalent to calcium concentration, the impurities werestill formed and got accumulated as black layer at the interphase oforganic and aqueous layers indicating that calcium naphthenate doeshydrolyze in presence of H₂S [or sulfur compound] and water, butDL-malic acid additive was also ineffective in avoiding formation ofimpurities, and thereby, in accumulation of black layer at theinterphase. The acid value of about 213.5 (mg KOH per gm) of separatedand dried organic layer, and no peak at 1538 cm⁻¹ and at 1680.7 cm⁻¹,but strong peak at 1699.8 cm⁻¹ in its IR spectra, as shown inaccompanying FIG. 7, were also indicative of hydrolysis of calciumnaphthenate. In the description herein, this experiment may be referredto as experiment 7.

When experiment 7 was repeated with concentration of H₂S in the vapourphase of about 5 vol % to see if DL-malic acid additive is effective toavoid formation of impurities and their accumulation at the interphase,it was found that even at lower concentration of 5 vol % of H₂S, theDL-malic acid additive was ineffective in avoiding formation ofimpurities and their accumulation at the interphase even when organiclayer has been treated for a period up to 60 min. In the descriptionherein, this experiment may be referred as experiment 7A. The calciumconcentration in the organic layer, as measured by ICP, and AV of thecompound obtained after drying the organic layer are provided againsttime in the Table-V, which indicate that DL-malic acid additive may beeffective in removing the calcium, but it has not been found to beeffective in avoiding formation of impurities and their accumulation atthe interphase even when hydrocarbon layer is treated for a period up to60 min:

TABLE V Sr. Acid Value % Efficiency Ca Conc. % Efficiency No. Time(MgKOH/gm) (by AV) (ppm) (by Ca) 1  5 min 197.69 85.9 55 97.55 2 15 min211.78 92.0 48 97.8 3 30 min 212.52 92.4 144 93.59 4 60 min 211.45 91.994 95.82

The experiment no. 6 was also repeated with prior art additives for 5vol % concentration of H₂S also, and was found that none of the priorart additives were capable of dissolving the already formed impuritiesor black layer at the interphase even for such a lower concentration ofH₂S. In the description herein, these experiments may be referred asexperiment 6A, 6B, 6C and 6D for prior art additive glycolic acid,DL-malic acid, maleic anhydride and citric acid respectively. Thecalcium concentration in the organic layer, as measured by ICP, and AVof the compound obtained after drying the organic layer are provided inthe Table-VI, which indicate that the prior art additives may beeffective in removing the calcium, but have not been found to beeffective in dissolving the already formed impurities or black layer atthe interphase:

TABLE VI % Ca % Expt. Prior art Acid Value Efficiency Conc. EfficiencyNo. Additive (MgKOH/gm) (by AV) (ppm) (by Ca) Observation 6A Glycolic192.39 83.7 337 85 Impurities/Black layer Acid does not disappear 6BDL-Malic 187.84 81.7 355 84.2 Impurities/Black layer Acid does notdisappear 6C Maleic 173.38 75.4 528 76.5 Impurities/Black layeranhydride does not disappear 6D Citric acid 218.0 94.7 112 95Impurities/Black layer does not disappear

The inventor has also observed that even if the prior art additives aretaken in double the stoichiometric equivalent of calcium concentration,none of these have been found to be effective in avoiding formation ofimpurities and their accumulation as black layer at the interphase. Inthe description herein, these experiments may be referred as experiment8A, 8B, 8C and 8D for prior art additive glycolic acid, DL-malic acid,maleic anhydride and citric acid respectively. The calcium concentrationin the organic layer, as measured by ICP, and AV of the compoundobtained after drying the organic layer are provided in the Table-VIIfor treatment duration of 5 min, which indicate that the prior artadditives may be effective in removing the calcium, but have not beenfound to be effective avoiding formation of impurities and theiraccumulation as black layer at the interphase:

TABLE VII % Ca % Expt. Prior art Acid Value Efficiency Conc. EfficiencyNo. Additive (MgKOH/gm) (by AV) (ppm) (by Ca) Observation 8A Glycolic205.45 89.3 112 95 Impurities/Black layer Acid does not disappear 8BDL-Malic 212.29 92.3 20 99.1 Impurities/Black layer Acid does notdisappear 8C Maleic 215.23 93.5 24 98.9 Impurities/Black layer anhydridedoes not disappear 8D Citric acid 225.24 97.9 12 99.46 Impurities/Blacklayer does not disappear

It is understood from the foregoing description that none of the priorart additives including citric acid (C3 alpha-hydroxy-tricarboxylicacid), maleic anhydride, glycolic acid and DL-Malic acid which may beeffective to remove metal including calcium from DOBA crude oil, areneither effective to avoid formation of impurities on account ofreaction between calcium naphthenate and sulfur compound or H₂S inpresence of water, nor effective to remove or dissolve the impuritieswhich are formed on account of reaction between calcium naphthenate andsulfur compound or H₂S in presence of water in mixture of crude oilscontaining calcium naphthenate and sulfur compound or H₂S.

Need of the Invention

Therefore, there is a need to have an additive which is effective notonly to avoid formation of impurities formed on account of reactionbetween calcium naphthenate and sulfur compound including H₂S inpresence of water, but also effective to remove or dissolve theimpurities which are formed on account of reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water inmixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S, and method thereof. Additionally, such additive should becapable of removing metal impurities including calcium from DOBA crudeoil.

Objects and Advantages of the Invention

Accordingly, the main object of the present invention is to provide anadditive which is effective not only to avoid formation of impuritieswhich would have formed on account of reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water, butis also effective to remove or dissolve the impurities which are formedon account of reaction between calcium naphthenate and sulfur compoundincluding H₂S in presence of water in mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S. Additionally, thepresent invention aims to provide an additive which is effecting inremoving metal including calcium from DOBA crude oil.

This is also an object of the present invention to provide a method toavoid formation of impurities which would have formed on reactionbetween calcium naphthenate and sulfur compound including H₂S inpresence of water in mixture of crude oils containing calciumnaphthenate and sulfur compound including H₂S.

This is also an object of the present invention to provide a method toremove or dissolve the impurities formed on reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water inmixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S.

This is also an object of the present invention to provide an additivewhich is effective to remove metals including calcium from crude oil ormixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S and simultaneously avoiding formation of impurities, andremoving or dissolving the impurities which are already formed, onaccount of reaction between calcium naphthenate and sulfur compoundincluding H₂S in presence of water in the crude oil or mixture of crudeoils containing calcium naphthenate and sulfur compound including H₂S.

It is also an object of the present invention to provide an additive andmethod of employing that additive which is effective not only to avoidformation of impurities, but is also effective to remove or dissolve theimpurities which, respectively, would have formed or are formed onaccount of reaction between calcium naphthenate and sulfur compoundincluding H₂S in presence of water in mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S even at pH of 7 ormore with addition of any additional mineral acid. Additionally, thepresent invention aims to provide an additive which is effecting inremoving metal including calcium from DOBA crude oil even at pH of 7 ormore.

Other objects and advantages of the present invention will become moreapparent when the following description is read in conjunction withfollowing examples and accompanying figures, which are not intended tolimit the scope of present invention.

BRIEF DESCRIPTION OF THE ACCOMPANYING FIGURES

FIG. 1 illustrates IR spectra of dried organic material obtained inexperiment 1 as described herein.

FIG. 2 illustrates IR spectra of dried organic material obtained inexperiment 2 as described herein.

FIG. 3 illustrates IR spectra of dried organic material obtained afteremploying additive—citric acid as described herein.

FIG. 4 illustrates IR spectra of dried organic material obtained afteremploying additive—maleic anhydride as described herein.

FIG. 5 illustrates IR spectra of dried organic material obtained afteremploying additive—glycolic acid being ineffective in avoiding formationof impurities as described herein.

FIG. 6 illustrates IR spectra of dried organic material obtained afteremploying additive—glycolic acid and being ineffective in dissolvingimpurities formed as described herein.

FIG. 7 illustrates IR spectra of dried organic material obtained afteremploying additive—DL-Malic acid being ineffective in avoiding formationof impurities as described herein.

FIG. 8 illustrates IR spectra of dried organic material obtained afteremploying additive of present invention—glyoxylic acid in accordancewith one of the preferred embodiments of the present invention and beingeffective in avoiding formation of impurities as described herein.

FIG. 9 illustrates IR spectra of dried organic material obtained afteremploying additive of present invention—glyoxylic acid in accordancewith one of the preferred embodiments of the present invention and beingeffective in removing or dissolving impurities formed as describedhereinabove.

DETAILED DESCRIPTION OF THE INVENTION

With aim to solve above-described industrial problem of the prior art,the inventor of present invention has found that when glyoxylic acid isemployed as an additive in processing of mixture of crude oilscontaining calcium naphthenate and sulfur compounds including H₂S inpresence of water, the impurities are surprisingly and unexpectedly notformed, and hence, no black layer is accumulated at the interphase oforganic and aqueous layers, and if impurities are formed thesesurprisingly and unexpectedly get disappeared or dissolved, and hence,the black layer formed at the interphase of organic and aqueous layerssurprisingly and unexpectedly get disappeared or dissolved.

Accordingly, the present invention relates to an additive capable ofavoiding formation of impurities, and capable of removing or dissolvingimpurities already formed and accumulated at the interphase of organicand aqueous layers on reaction between calcium naphthenate and sulfurcompound including H₂S in presence of water in mixture of crude oilscontaining calcium naphthenate and sulfur compound including H₂S,wherein the additive is glyoxylic acid.

In one embodiment, the present invention relates to an additive capableof avoiding formation of impurities on reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water inmixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S, wherein the additive is glyoxylic acid.

In another embodiment, the present invention relates to an additivecapable of removing or dissolving impurities already formed on reactionbetween calcium naphthenate and sulfur compound including H₂S inpresence of water and accumulated at the interphase of organic andaqueous layers in mixture of crude oils containing calcium naphthenateand sulfur compound including H₂S, wherein the additive is glyoxylicacid.

In still another embodiment, the present invention relates to a methodfor avoiding formation of impurities, and for removing or dissolvingimpurities already formed and accumulated at the interphase of organicand aqueous layers on reaction between calcium naphthenate and sulfurcompound including H₂S in presence of water in mixture of crude oilscontaining calcium naphthenate and sulfur compound including H₂S,comprising step of treatment of mixture of crude oils containing calciumnaphthenate and sulfur compound including H₂S with glyoxylic acid.

In one embodiment, the present invention relates to a method foravoiding formation of impurities on reaction between calcium naphthenateand sulfur compound including H₂S in presence of water in mixture ofcrude oils containing calcium naphthenate and sulfur compound includingH₂S, comprising step of treatment of mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S with glyoxylicacid.

In another embodiment, the present invention relates to a method forremoving or dissolving impurities already formed and accumulated at theinterphase of organic and aqueous layers on reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water inmixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S, comprising step of treatment of mixture of crude oilscontaining calcium naphthenate and sulfur compound including H₂S withglyoxylic acid.

In yet another embodiment, the present invention relates to a anadditive which is effective to remove metals including calcium fromcrude oil or mixture of crude oils containing calcium naphthenate andsulfur compound including H₂S, and simultaneously effective in avoidingformation of impurities, and removing or dissolving the impurities whichare already formed and accumulated at the interphase of organic andaqueous layers, on account of reaction between calcium naphthenate andsulfur compound including H₂S in presence of water in the crude oil ormixture of crude oils containing calcium naphthenate and sulfur compoundincluding H₂S, wherein the additive is glyoxylic acid.

In further embodiment, the present invention relates to a method toremove metals including calcium from crude oil or mixture of crude oilscontaining calcium naphthenate and sulfur compound including H₂S, andsimultaneously to avoid formation of impurities, and to remove ordissolve the impurities already formed and accumulated at the interphaseof organic and aqueous layers on account of reaction between calciumnaphthenate and sulfur compound including H₂S in presence of water inthe crude oil or mixture of crude oils containing calcium naphthenateand sulfur compound including H₂S, comprising treating the mixture ofcrude oils containing calcium naphthenate and sulfur compound includingH₂S with glyoxylic acid.

In accordance with present invention, a method for avoiding formation ofimpurities on reaction between calcium naphthenate and sulfur compoundincluding H₂S in presence of water in mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S, comprisesaddition of additive glyoxylic acid before separating organic andaqueous phases which surprisingly does not allow formation of impuritieswhich otherwise would have formed and got accumulated at the interphaseof organic and aqueous phases as a black layer and hampered processingof crude oils and removal of metals including calcium.

Therefore, the additive and method of present invention have advantageof avoiding formation of impurities on account of reaction betweencalcium naphthenate and sulfur compound including H₂S in presence ofwater, and hence, accumulation thereof as black layer at the interphase,which means processing of crude oils containing calcium naphthenate andsulfur compounds including H₂S and removal of metals including calciumtherefrom becomes easier even in presence of water by employing additiveand method of present invention.

In accordance with present invention, a method for removing ordissolving impurities formed and accumulated at the interphase oforganic and aqueous layers on reaction between calcium naphthenate andsulfur compound including H₂S in presence of water in mixture of crudeoils containing calcium naphthenate and sulfur compound including H₂Scomprises addition of additive glyoxylic acid after the impurities haveformed which surprisingly and unexpectedly removes or dissolves theimpurities formed, and hence, removes or dissolves the black layeraccumulated at the interphase of organic and aqueous phases, whichotherwise would have hampered processing of crude oils and removal ofmetals including calcium.

Therefore, the additive and method of present invention also haveadvantage of removing or dissolving already formed impurities on accountof reaction between calcium naphthenate and sulfur compound includingH₂S in presence of water, and hence, removing or dissolving alreadyaccumulated black layer at the interphase, which means processing ofcrude oils containing calcium naphthenate and sulfur compounds includingH₂S and removal of metals including calcium therefrom becomes easiereven in presence of water by employing additive and method of presentinvention.

In accordance with one of the preferred embodiments of the presentinvention, a method for removing or dissolving impurities already formedand accumulated at the interphase of organic and aqueous layers onreaction between calcium naphthenate and sulfur compound including H₂Sin presence of water in mixture of crude oils containing calciumnaphthenate and sulfur compound including H₂S comprises addition ofadditive glyoxylic acid after the impurities have formed and accumulatedat the interphase of organic and aqueous layers, and the aqueous layerhas pH of 7 or more, which surprisingly and unexpectedly removes ordissolves the impurities formed even if pH of aqueous layer was 7 ormore, and hence, removes or dissolves the black layer accumulated at theinterphase of organic and aqueous phases, which otherwise would havehampered processing of crude oils and removal of metals includingcalcium.

Therefore, the additive and method of present invention also haveadvantage of removing or dissolving already formed impurities on accountof reaction between calcium naphthenate and sulfur compound includingH₂S in presence of water, and hence, removing or dissolving alreadyaccumulated black layer at the interphase even if pH of aqueous layer is7 or more, preferably the pH of aqueous layer is between 7 to 9, whichmeans processing of crude oils containing calcium naphthenate and sulfurcompounds including H₂S and removal of metals including calciumtherefrom becomes easier even in presence of water and at pH of 7 ormore, preferably pH of 7 to 9 by employing additive and method ofpresent invention.

In accordance with one of the preferred embodiments of the presentinvention, the pH of aqueous layer varies from 7 to 9.

In accordance with preferred embodiment of the present invention,glyoxylic acid additive may be added either along with water or afterdissolving in water.

In accordance with preferred embodiment of the present invention, theglyoxylic acid additive may be added in a stoichometric or a doublestoichometric equivalent to calcium concentration, however no specialbenefit is seen when glyoxylic acid additive is added in doublestoichometric amount with reference to calcium concentration, whichmeans present additive and its method of employing are economical. Acare is to be taken that present additive is added either instoichometric amount or little excess with respect to calciumconcentration.

Therefore, it has been observed that when glyoxylic acid additive ofpresent invention is employed, not only formation of impurities isavoided or formed impurities are removed or dissolved, but furtherprocessing of crude oils also becomes surprisingly and unexpectedlyeasier resulting in removal of metals including calcium with ease andeconomically.

In accordance with one of the preferred embodiments of the presentinvention, the glyoxylic acid is identifiable by cas no. 298-12-4.

In accordance with another preferred embodiment of the presentinvention, the glyoxylic acid may also be referred to as oxo aceticacid.

The present invention is now explained with the help of followingexamples, which have been incorporated for explaining its best mode andare not intended to limit its scope.

EXAMPLES

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in above experiment 2 was treated in same manner as inexperiment 2, but with equal weight of water containing additive ofpresent invention—glyoxylic acid in stoichometric equivalent to calciumconcentration, surprisingly and unexpectedly no impurities were formed,and hence, no black layer was accumulated at the interphase of organicand aqueous layers indicating that calcium naphthenate did hydrolyze inpresence of H₂S [or sulfur compound] and water, but glyoxylic acidadditive was effective in avoiding formation of impurities, and thereby,in accumulation of black layer at the interphase. The acid value ofabout 230.01 (mg KOH per gm) of separated and dried organic layer, andno peak at 1538 cm⁻¹ and at 1680.7 cm⁻¹, but strong peak at 1698.6 cm⁻¹in its IR spectra, as shown in accompanying FIG. 8, were also indicativeof hydrolysis of calcium naphthenate. In the description herein, thisexperiment may be referred to as experiment 9. This experiment confirmsthat additive of present invention—glyoxylic acid is effective inavoiding formation of impurities which otherwise would have gotaccumulated as black layer at the interphase and hampered processing ofcrude oils containing calcium naphthenate and sulfur compounds includingH₂S.

When experiment 9 was repeated for different intervals withconcentration of H₂S in the vapour phase of about 5 vol % by employingadditive of present invention—glyoxylic acid, no black layer was formedat 5, 15, 30 and 60 min intervals confirming that present additive waseffective in avoiding formation of impurities and thereby accumulationof black layer at the interphase even after treatment of 5 min. Thecalcium content in the organic phase, as determined by ICP, was found tobe as low as 12, 9, 6 and 3 ppm respectively for 5, 15, 30 and 60 minintervals confirming 99.5%, 99.6%, 99.7% and 99.9% efficiency of presentadditive—glyoxylic acid to remove calcium. The data including the acidvalue (AV) of the dried organic material is summarized in Table VIII.

TABLE VIII % Ca % Sr. Acid Value Efficiency Conc. Efficiency No Time(MgKOH/gm) (by AV) (ppm) (by Ca) Observation 1  5 min 218.49 95.0 1299.5 No impurities or black layer at the interphase 2 15 min 227.19 98.89 99.6 No impurities or black layer at the interphase 3 30 min 219.5995.5 6 99.7 No impurities or black layer at the interphase 4 60 min223.0 96.9 3 99.9 No impurities or black layer at the interphase

It is observed from Table VIII that calcium naphthanate hydrolysesalmost completely just in 5 min, since 95% efficiency by acid value isobtained along with 99.5% efficiency by calcium removal, and theseefficiencies were found to be 96.9% and 99.9% respectively at 60 mininterval.

When solution of calcium naphthenate in toluene and purged with H₂S asprepared in experiment 2 was treated in same manner as in experiment 2with equal weight of water, the impurities were formed and gotaccumulated as dense black layer at the interphase indicating thatcalcium naphthenate does hydrolyze in presence of H₂S [or sulfurcompound] and water. The aqueous layer was carefully drained andadditive—glyoxylic acid in stoichometric equivalent to calciumconcentration was dissolved in this separated aqueous layer, which isthen transferred back to the separating funnel containing organic andblack layers, and the contents were vigorously shaken. It was observedthat black layer formed surprisingly and unexpectedly get disappeared ordissolved, which confirms that additive glyoxylic acid was effective inremoving or dissolving the impurities which had got accumulated as blacklayer at the interphase. The acid value of about 227.82 (mg KOH per gm)of separated and dried organic layer, and no peak at 1538 cm⁻¹ and at1680.7 cm⁻¹, but strong peak at 1699.1 cm⁻¹ in its IR spectra, as shownin accompanying FIG. 9, were also indicative of hydrolysis of calciumnaphthenate. In the description herein, this experiment may be referredto as experiment 10. It may be noted that this experiment was alsoperformed by direct addition of aqueous solution of additive glyoxylicacid after accumulation of black layer at the interphase, instead ofseparating aqueous layer and dissolving the additive therein andtransferring back to separating funnel, and surprisingly it was foundthat black layer gets disappear or dissolved indicating that glyoxylicacid was effective in removing or dissolving black layer formed byaccumulation of impurities at the interphase.

In above experiments, for the concentration of 5 vol. % of H₂S, the pHof aqueous layer after separation was fond to be varying between 7 to 8,preferably between 7.10 to 7.50, and for the concentration of 13 vol. %of H₂S, the pH of aqueous layer after separation was fond to be varyingbetween 8 to 9, preferably between 8.10 to 7.50.

As in above experiments, the glyoxylic acid has been found to beeffective in removing or dissolving the impurities, and hence, blacklayer already formed at the interphase on account of reaction betweencalcium naphthenate and sulfur compounds including H₂S, it can beconcluded that additive of present invention is also effective inremoving or dissolving already formed impurities, and hence, black layeralready formed at the interphase even if pH of aqueous layer is 7 ormore, preferably the pH of aqueous layer is between 7 to 9, which meansprocessing of crude oils containing calcium naphthenate and sulfurcompounds including H₂S and removal of metals including calciumtherefrom becomes easier even in presence of water and at pH of 7 ormore, preferably pH of 7 to 9 by employing additive and method ofpresent invention.

The above experiments confirm that solution to the industrial problemsof processing mixture of DOBA or its blend containing calciumnaphthenate and a crude oil containing sulfur compounds including H₂Sdue to formation of impurities or possibility of formation of impuritiesupon reaction between calcium naphthenate and sulfur compounds includingH₂S on contact with water has been provided, and hence, processing ofsuch mixtures of crude oils as well as removal of metals includingcalcium therefrom becomes easier and economical.

It may be noted that present invention has been described with the helpof foregoing experiments which have been performed on the laboratoryscale. It is obvious to persons skilled in the art to modify presentinvention to apply it to industrial scale without deviating from itsscope.

1-3. (canceled)
 4. An additive capable of removing metals includingcalcium from crude oil or mixture of crude oils containing calciumnaphthenate and sulfur compound including H₂S, and simultaneouslycapable of avoiding formation of impurities and removing the impurities,if already formed and accumulated at the interphase of organic andaqueous layers, characterized in that said impurities are formed onaccount of reaction between calcium naphthenate and sulfur compoundincluding H₂S in presence of water in mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S, wherein theadditive is glyoxylic acid. 5-7. (canceled)
 8. A method to remove metalsincluding calcium from crude oil or mixture of crude oils containingcalcium naphthenate and sulfur compound including H₂S, andsimultaneously to avoid formation of impurities and to remove theimpurities, if already formed and accumulated at the interphase oforganic and aqueous layers, characterized in that said impurities areformed on account of reaction between calcium naphthenate and sulfurcompound including H₂S in presence of water in the crude oil or mixtureof crude oils containing calcium naphthenate and sulfur compoundincluding H₂S, comprising treating the said mixture of crude oilscontaining calcium naphthenate and sulfur compound including H₂S withglyoxylic acid.
 9. A method as claimed in claim 8, wherein for avoidingformation of impurities the additive is added before separating organicand aqueous phases.
 10. A method as claimed in claim 8, wherein forremoving the impurities already formed comprises addition of additiveglyoxylic acid after the impurities have formed.
 11. A method as claimedin claim 8, wherein pH of aqueous layer is 7 or more.
 12. A method asclaimed in claim 11, wherein pH of aqueous layer varies from 7 to
 9. 13.A method as claimed in claim 8, wherein the additive is added eitheralong with water or after dissolving in water.
 14. A method as claimedin claim 8, wherein the additive is added in a stoichometric or a doublestoichometric equivalent to calcium concentration.
 15. A method asclaimed in claim 8, wherein the additive is added either instoichometric amount or little excess with respect to calciumconcentration. 16-18. (canceled)